Lower Glycated Hemoglobin with Real-Time Continuous Glucose Monitoring Than with Intermittently Scanned Continuous Glucose Monitoring After 1 Year: The CORRIDA LIFE Study
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F44555601%3A13430%2F22%3A43897486" target="_blank" >RIV/44555601:13430/22:43897486 - isvavai.cz</a>
Alternative codes found
RIV/00216208:11110/22:10448082
Result on the web
<a href="https://www.liebertpub.com/doi/full/10.1089/dia.2022.0152" target="_blank" >https://www.liebertpub.com/doi/full/10.1089/dia.2022.0152</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1089/dia.2022.0152" target="_blank" >10.1089/dia.2022.0152</a>
Alternative languages
Result language
angličtina
Original language name
Lower Glycated Hemoglobin with Real-Time Continuous Glucose Monitoring Than with Intermittently Scanned Continuous Glucose Monitoring After 1 Year: The CORRIDA LIFE Study
Original language description
Background: The aim was to compare the efficacy of real-time continuous glucose monitoring (rtCGM) and intermittently scanned continuous glucose monitoring (isCGM) focusing on glycated hemoglobin (HbA1c) as the primary endpoint.Methods: The CORRIDA LIFE was a 12-month, real-world, nonrandomized study that is part of the CORRIDA clinical trials program. The study compared rtCGM (Dexcom G5 or G6) and isCGM (FreeStyle Libre 14-Day; Abbott) in adults with type 1 diabetes (T1D). Only patients on multiple daily insulin injections or continuous subcutaneous insulin infusion with no automatic functions were included in this study. Primary outcome was the difference in HbA1c between study groups at 12 months.Results: One hundred ninety-one adults with T1D (mean age 40 +/- 13 years, HbA1c 8.1% +/- 3.4% [65 +/- 14 mmol/mol]) participated in this study; 81 patients initiated rtCGM and 110 initiated isCGM. After 12-months, HbA1c was significantly lower with rtCGM versus isCGM (7.1% +/- 3.1% [54.1 +/- 10.1 mmol/mol] vs. 7.7% +/- 3.3% [61.2 +/- 12.2 mmol/mol]), P = 0.0001. The percentage of time in hypoglycemia (<70 mg/dL [<3.9 mmol/L]) was lower among rtCGM vs. isCGM participants [4.3% +/- 2.8% vs. 6.4% +/- 5.3%], P = 0.003). Patients with rtCGM spent less time in clinically significant hypoglycemia (<54 mg/dL [<3.0 mmol/L]) (0.9% +/- 1.0% vs. 2.3% +/- 2.5%, P < 0.0001) and more time in target range (70-180 mg/dL [3.9-10 mmol/L]) than isCGM users (67.5% +/- 14.8% vs. 57.8% +/- 17.0%), P = 0.0002.Conclusions: rtCGM was superior to isCGM in HbA1c, hypoglycemia, and other glycemic outcomes. Our findings provide guidance to clinicians when discussing monitoring options with their patients. The study was registered at www.clinicaltrials.gov (NCT04759495).
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
30304 - Public and environmental health
Result continuities
Project
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Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2022
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
DIABETES TECHNOLOGY & THERAPEUTICS
ISSN
1520-9156
e-ISSN
1557-8593
Volume of the periodical
24
Issue of the periodical within the volume
12
Country of publishing house
US - UNITED STATES
Number of pages
9
Pages from-to
859-867
UT code for WoS article
000892073400001
EID of the result in the Scopus database
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